[血管性behaperet病1例,最初表现为b rger病样血管粥样硬化]。

Ryumachi. [Rheumatism] Pub Date : 2003-10-01
Masashi Takebayashi, Yoshio Ozaki, Yonsu Son, Minori Nagahama, Shirou Fukuhara
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引用次数: 0

摘要

患者是一名24岁的男性。b rger病最初是基于发现双侧桡动脉阻塞而诊断的,患者接受了血管重建手术。然而,手术后,在肘部的左肱动脉中经常观察到假性动脉瘤的形成,这需要总共进行多达5次血管重建手术,包括在调查过程中多次穿刺的右股总动脉。临床过程中出现发热、口腔溃疡、生殖器溃疡、结节性红斑,诊断为不完全性behaperet病。组织病理学检查显示血管病变符合坏死性脉管炎。全身性炎症和血管炎在类固醇治疗后得到改善。血管性behet病是一种特殊类型的behet病,但通常发生在病史较长的患者身上。我们的病人被认为是很有指导意义的,因为当behet病并发脉管炎并且流行病学特征与我们的病人一样的b rger病一致时,鉴别可能很困难。
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[Case of vascular Behçet's disease initially presented with Bürger's disease-like vasculitides].

The patient was a 24-year-old man. Bürger's disease was diagnosed initially based on the finding of bilateral radial artery obstruction, and the patient underwent vascular reconstructive surgery. After the operation, however, formation of false aneurysms was observed frequently in the left brachial artery at the elbow, which necessitated performance of vascular reconstructive surgery up to five times in total, including of the right common femoral artery, which had been punctured several times for investigational procedures. During the clinical course, fever, oral aphthoid ulcers, genital ulcers, and nodular erythema appeared, and incomplete Behçet's disease was diagnosed. Histopathological examination suggested that the vascular lesion was consistent with necrotizing angiitis. The systemic inflammatory findings and angiitis improved following steroid administration. Vascular Behçet's disease is known as a special type of Behçet's disease, but usually develops in the patients with a long history of the disease. Our patient was believed to be very instructive because, when Behçet's disease occurs with angiitis and the epidemiological characteristics agree with those of Bürger's disease like in our patient, differentiation may be difficult.

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